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Of adrenergic

Prazosin, a selective a -adrenoceptor antagonist, exerts its antihypertensive effect by blocking the vasoconstrictor action of adrenergic neurotransmitter, norepinephrine, at a -adrenoceptors in the vasculature (200,227,228). Prazosin lowers blood pressure without producing a marked reflex tachycardia. It causes arteriolar and venular vasodilation, but a significant side effect is fluid retention. Prazosin increases HDL cholesterol, decreases LDL cholesterol, and does not cause glucose intolerance. [Pg.141]

Alteration of the structural pattern produces a pair of adrenergic a-blocking agents which serve as anti hypertensives. These structures are reminiscent of prazoci n. Reaction of piperazine with 2-furoy1 chloride followed by catalytic reduction of the furan ring leads to synthon 69. This, when heated... [Pg.194]

An imidazole derivative which is also a hypotensive agent by virtue of adrenergic a-2-receptor blockade is imiloxan (75). Its synthe.sis begins by conversion of 2-cyanomethyl-1,4-benzodioxane (72) to its iminosMhylether with anhydrous HC in clhanol (73). Reaction of the latter with aminoacetaldehyde diethylacetal and subsequent acid treatment produces the imidazole ring (74). Alkylation of 74 with ethyl iodide mediated by sodium hydride completes the synthesis [251. [Pg.88]

Noradrenaline transporters (NAT) are localized in the presynaptic plasma membrane of adrenergic nerve terminals. They belong to a family of proteins with 12 putative transmembrane proteins which are responsible for recycling of released neurotransmitters (noradrena-line/adrenaline, dopamine, serotonin, amino acid transmitters) back into the presynaptic nerve ending. Noradrenaline transporters can be blocked by a number of different antidepressant drags, including tricyclic antidepressants (e.g. desipramine) and selective noradrenaline reuptake inhibitors (e.g. reboxetine). [Pg.883]

Discuss the types of shock, physiologic responses of shock, and the use of adrenergic drugs in the treatment of shock. [Pg.199]

Discuss the uses, general drug actions, contraindications, precautions, interactions, and adverse reactions associated with the administration of adrenergic drugs. [Pg.199]

Discuss ways to promote an optimal response to therapy, how to manage common adverse reactions, and important points to keep in mind when educating patients about the use of adrenergic drugs. [Pg.199]

List the four types of adrenergic blocking drugs. [Pg.210]

A new nurse says that she is unsure about how the adrenergic blocking drugs work. Discuss the four types of adrenergic blocking drugs and how each one works within the body. [Pg.219]

The initial component of the PTX-induced contraction is selectively inhibited by ouabain, whereas the second component is rather potentiated by it (77). A similar inhibitory effect of ouabain on the contractile response to PTX is observed in the umbilical artery, which is devoid of adrenergic innervation 18). [Pg.222]

Trazodone routinely causes sedation, which is why it is used far more often as an adjunct with other antidepressants for sleep than as a primary agent for the treatment of depression. Priapism is a rare but serious adverse effect in males who take trazodone. In addition, orthostatic hypotension and dizziness are more common with trazodone than with nefazodone because the latter agent has a weaker effect at a-adrenergic receptors and also has a balancing of adrenergic effects owing... [Pg.574]

Sympathetic stimulation of adrenergic receptors on the granular cells of the juxtaglomerular apparatus promotes secretion of renin and, consequently, formation of angiotensin II. Angiotensin II then causes ... [Pg.337]

Of the many types of adrenergic receptors found throughout the body, which is most likely responsible for the cardiac stimulation that is observed following an intravenous injection of epinephrine ... [Pg.170]

Inhibition of adenylyl cyclase by mAChR activation results in decreased cAMP formation. A decrease in cAMP is most apparent when adenylyl cyclase is stimulated, for example, by activation of adrenergic receptors... [Pg.203]

Virkki, L. and M. Nikinmaa. 1993. Tributyltin inhibition of adrenergically activated sodium/proton exchange in erythrocytes os rainbow trout (Oncorhynchus mykiss). Aquat. Toxicol. 25 139-146. [Pg.634]

The major types of adipose tissue are (1) white adipose tissue, which manufactures, stores, and releases lipid and (2) brown adipose tissue, which dissipates energy via uncoupled mitochondrial respiration. Obesity research includes evaluation of the activity of adrenergic receptors and their effect on adipose tissue with respect to energy storage and expenditure or thermogenesis. [Pg.676]

Corticosteroids increase the number of / -adrenergic receptors and improve receptor responsiveness to /f2-adrenergic stimulation, thereby reducing... [Pg.926]


See other pages where Of adrenergic is mentioned: [Pg.141]    [Pg.358]    [Pg.359]    [Pg.23]    [Pg.139]    [Pg.2]    [Pg.858]    [Pg.200]    [Pg.204]    [Pg.210]    [Pg.210]    [Pg.624]    [Pg.134]    [Pg.713]    [Pg.713]    [Pg.714]    [Pg.714]    [Pg.313]    [Pg.57]    [Pg.637]    [Pg.105]    [Pg.101]    [Pg.137]    [Pg.20]    [Pg.184]    [Pg.178]    [Pg.220]    [Pg.221]    [Pg.221]    [Pg.854]    [Pg.492]    [Pg.495]   


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